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accuracy: The closeness of a measured volume to the true volume as specified by the volume setting of the pipette. Also known as “mean error”.
precision: The closeness of agreement among the individual weighings. Also known as standard deviation, reproducibility and repeatability.
Pipetting errors
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PCRPolymeraseChainReaction
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A concept similar to that of PCR had been described before Mullis' work. Nobel Prize laureate H. Gobind Khorana and Kjell Kleppe, a Norwegian scientist, authored a paper seventeen years earlier describing a process they termed "repair replication" in the Journal of Molecular Biology.
Wikipedia
Kary Mullis developed the PCR method in 1983 and received the Nobel price for this in 1993.
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PCR allows the amplification of specific fragments of DNA:
You need some sequence information of what you are going to amplify because primers are sequence specific.
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PCR Movies
http://www.youtube.com/watch?v=j9Gu7iwBi4Ihttp://www.dnalc.org/resources/animations/pcr.html
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5'
3'
DNA polymerization occurs from 5' to 3'
http://web.virginia.edu/Heidi/chapter30/chp30.htm
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Reaction components:
94C 94C
40-70C
72C 72C
x20-30
DenaturationAnnealing
Elongation
A typical PCR reaction has 3 steps
Polymerase (e.g. Taq polymerase from Thermus aquaticusMg2+
dNTPsTemplatePrimers
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What are the factors affecting:
Annealing temperature
Elongation time
primer length, primer GC content, salt concentration
enzyme processivity, fragment length
(Taq polymerase has an extension rate of 35-100 nt/sec)
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unspecific hybridization of primerspolymerase mistakesDNA contamination
PCR problems
When would you get no product?
One or more components missingWrong annealing temperatureElongation temperature is too short
When would you get the wrong product?
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Uses of PCR
CLONING:amplifying DNA fragments for further processingmutating DNA fragments: addition of nucleotides
exchange of nucleotidesamplifying homologous DNA fragments
DETECTION:quantifying DNA: real time PCRmapping mutations: point mutations
insertions/deletions